用激光诱导击穿光谱技术比较土豆和百合中的微量元素

激光诱导击穿光谱(LIBS)已成功地运用于固体、液体、气体样品中微量元素的测量以及微生物、细菌等的鉴别分析上,而在植物样品上面的应用则是一个较新的课题。该实验用纳秒Nd:YAG激光器击穿真空冻干的土豆、百合样品,用光纤光谱仪测量了其LIBS光谱。通过鉴别、分析LIBS光谱,得到了这两种样品中微量元素的成分。并且对土豆干和百合干中Ca,Na,K,Fe,Al,Mg六种金属元素典型谱线的强度进行了统计分析,并由此得到了样品中这六种微量元素含量的对比情况。实验结果表明土豆干中的Ca和Na等含量都明显高于百合干,而百合干中Mg的含量较高。实验结果还表明用LIBS技术检测、对比冻干植物样品中微量元素含量是一种快速、有效的分析方法。

CSRe团簇内靶的真空与分子泵监测系统的设计

介绍了国家重大科学工程项目——兰州重离子加速器冷却存储环(HIRFL-CSR)的实验环(CSRe)团簇内靶真空与分子泵监测系统。该系统主要通过一个应用程序获取各真空规及分子泵的状态值,并存入、更新Oracle数据库。浏览器上的ActiveX从Oracle中读取各设备状态值进行显示,如果状态值在警戒范围,则做出相应的控制操作。该系统在实验测试中运行良好,能满足实验的要求。

Microelements in Potato and Lily Samples Studied by Laser-Induced Breakdown spectroscopy Technology

A LIBS setup was built in the Institute of Modern Physics. In our experiments, LIBS spectra produced by infrared radiation of Nd : YAG nanosecond laser with 100 and 150 mJ pulse energy, respectively, were measured by fiber optic spectrometer in the ranges of 230-430 run and 430-1080 nm with a delay time of 1.7 and gate width of 2 ms for potato and lily samples prepared by vacuum freeze-dried technique. The lines from different metal elements such as K, Ca, Na, Mg, Fe, Al, Mn and Ti, and nonmetal elements such as C, N, O and H, and some molecular spectra from C-2, CaO, and CN were identified according to their wavelengths. The relative content of the six microelements, Ca, Na, K, Fe, Al, and Mg in the samples were analyzed according to their representative line intensities. By comparison we found that there are higher relative content of Ca and Na in lily samples and higher relative content of Mg in potato samples. The experimental results showed that LIBS technique is a fast and effective means for measuring and comparing the contents of microelements in plant samples.

科学管理人类智慧的宝库──关于加强文献资源共建共享基本模式的初探

科学管理人类智慧的宝库──关于加强文献资源共建共享基本模式的初探梁伟（中国科学院沈阳应用生态所）自有文字以来，文献资源的积累就是人类智慧的巨大宝库。过去，一个人若要完全占有这个宝库，视天下文献资源为己所藏，为我所用，恐怕会被人笑为是狂人的幻想，而今这...

非工程措施在灾害防治中的重要作用

分析研究了灾害的危害和非工程措施在国民经济发展中的地位与作用 ,因地制宜的提出了几条防灾对策。

旱作高产田产量波动性和土壤干燥化

根据旱地作物长期田间试验数据 ,论述了旱作农业生产中作物产量波动性是一个规律性现象 ,并用波动系数加以表述。研究结果表明旱作高产田与低产田相比 ,存在相似的产量波动性 ,区别是它在较高产量水平上波动。高产田作物耗水量较高 ,从而导致土壤相对干燥化。土壤干燥化是高产田产量产生波动性的直接原因 ;而低产田则因作物吸水能力低 ,土壤储水不能充分利用所致

Distribution characteristics of (CS)-C-137 in wind-eroded soil profile and its use in estimating wind erosion modulus

Due to its inert reaction in soil system and distinctive vertical distribution in soil profile, caesium-137 (Cs-137) has been used as a tracer to assess wind erosion. In this study, 62 soil samples were collected from 4 sampling sites in Taipusi County, Inner Mongolia; Caesium-137 activities for those soil samples were measured using a gamma-ray spectrometry in Sichuan University, Chengdu. Distribution pattern of Cs-137 in vertical soil profile was different for different land use and land cover types. Caesium-137 was distributed homogeneously in plow layer of cropland, and negatively exponential in low to medium cover grassland. Distribution pattern in high covered grassland was represented by a peak at 2-4 cm soil depth followed by a negative exponential curve. Based on those findings, simplified mass balance model was chosen to estimate the rate of wind erosion for cropland, while profile distribution model was used for grassland. Estimated wind erosion rates were 7990, 4270 and 1808 Mg(.)km(-2.)a(-1) for cropland, low cover grassland and medium cover grassland, respectively. Wind erosion intensity correlated negatively with plant cover.

Hydrogen peroxide biosensor based on direct electrochemistry of soybean Peroxidase immobilized on single-walled carbon nanohorn modified electrode

Single-walled carbon nanohorns (SWCNHs) were used as a novel and biocompatible matrix for fabricating biosensing devices. The direct immobilization of acid-stable and thermostable soybean peroxidase (SBP) on SWCNH modified electrode surface can realize the direct electrochemistry of enzyme. Cyclic voltammogram of the adsorbed SBP displays a pair of redox peaks with a formal potential of -0.24V in pH 5 phosphate buffer solution.

A Simple, Universal Colorimetric Assay for Endonuclease/Methyltransferase Activity and Inhibition Based on an Enzyme-Responsive Nanoparticle System

An enzyme responsive nanoparticle system that uses a DNA-gold nanoparticle (AuNP) assembly as the substrate has been developed for the simple, sensitive, and universal monitoring of restriction endonucleases in real time. This new assay takes advantage of the palindromic recognition sequence of the restriction nucleases and the unique optical properties of AuNPs and is simpler than the procedure previously described by by Xu et al. (Angew. Chem. Int. Ed. Engl. 2007, 46, 3468-3470). Because it involves only one type of ssDNA modified AuNPs, this assay can be directed toward most of the endonucleases by simply changing the recognition sequence found within the linker DNA. In addition, the endonuclease activity could be quantitatively analyzed by the value of the reciprocal of hydrolysis half time (t(1/2)(-1). Furthermore, our new design could also be applied to the assay of methyltransferase activity since the methylation of DNA inhibits its cleavage by the corresponding restriction endonuclease, and thus, this new methodology can be easily adapted to high-throughput screening of methyltransferase inhibitors.

纳米AgBr/PMMA光致变色杂化材料制备与表征

采用本体聚合法制备了纳米AgBr/PMMA(聚甲基丙烯酸甲酯)光致变色杂化材料.XRD分析表明,纳米AgBr/PMMA杂化材料是无定形的.SEM分析表明,AgBr含量不同,杂化材料的断面形貌明显不同,随AgBr含量的增加,杂化材料由韧性断裂向脆性断裂转变.EDS面分析表明,Ag、Br元素在杂化材料中均匀分布.所制备的纳米AgBr/PMMA杂化材料具有一定的光致变色效应.

Solvothermal synthesis of the complex fluorides KMgF3 and KZnF3 with the Perovskite structures

The complex fluorides KMgF3 and KZnF3 with Perovskite structures were solvothermally synthesised at 150-180degreesC and characterised by means of X-ray powder diffraction, scanning electron microscopy, thermogravimetric analysis and infrared spectroscopy.

Voltammetric behavior of tetracine on glassy garbon electrode and its application

The anodic voltammetric behavior of anaesthetic tetracine and its application were studied. In 0.1 mol/L HClO4 solution, the potential of anodic peak for tetracine is 1.04 V(vs. Ag/AgCl) at a glassy carbon electrode. A linear relationship between the peak height and the concentration of tetracine in the range of 5 x 10(-4) similar to 1 x 10(-1) g/L was obtained. The peak current decreases with the decreasing acidity of the solution. the mehtod has been used for the direct determination of tetracine in injections. The average recoveries of tetracine in urine samples were 98.5%. The mechanism of the electrode reaction was also discussed.

Electrospray ionization multiple-stage tandem mass spectrometric analysis of diglycosyldiacylglycerol glycolipids from the bacteria Bacillus pumilus

Electrospray ionization (ESI) combined with multiple-stage tandem mass spectrometry (MSn) was used to directly analyze the glycolipid mixture from bacteria Bacillus pumilus without preliminary separation. Full scan ESI-MS revealed the composition of picomole quantities of glycerolglycolipid species containing C-14-C-19 fatty acids, some of which were monounsaturated, Two main components were identified from their molecular masses and fragmentation pathways. The fragmentation pathway of the known compound compared with the investigated compound verified the proposed structure as 1(3)-acyl-2-pentadecanoyl-3(1)-O-[beta-D-glucopyranosyl-(1-->6)-O-beta-D-glucopyranosyl]-sn-glycerols. A comparison of the multiple tandem mass spectra of the different alkali-metal cation adducts indicates that the intensity of fragments and the dissociation pathways are dependent on the alkali-metal type, The basic structures of glycerolglycolipids were reflected clearly from the fragmentation patterns of the sodium cations, The intense fragments of the sugar residue from the precursor ions were obtained from the lithiated adduct ions. ESI-MSn spectra of [M + K](+) ions did not provide as much fragmentation as [M + Na](+) and [M + Li](+) adducts, but their spectra allow the position of glycerol acylation to be determined. On the basis of MS2 spectra of[M + K](+) ions, it was established that all components have a C-15:0 fatty acid at the sn-2 position of the glycerol backbone and C-14-C-19 acids at the sn-1 position of the glycerol backbone. Copyright (C) 1999 John Wiley & Sons, Ltd.